Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23413809C>ACA389034576MYH7c.5740G>T (p.Glu1914Ter)
ClinVar dbSNP
14g.23413809C=CA2123458197MYH7c.5740G= (p.Glu1914=)
14g.23413809C>GCA389034577MYH7c.5740G>C (p.Glu1914Gln)
14g.23413809C>TCA016441MYH7c.5740G>A (p.Glu1914Lys)
ClinVar dbSNP
14g.23413810G>ACA016434MYH7c.5739C>T (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413810G>CCA048139MYH7c.5739C>G (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413810G=CA2123458210MYH7c.5739C= (p.Ala1913=)
14g.23413810G>TCA485616117MYH7c.5739C>A (p.Ala1913=)
dbSNP
14g.23413811G>ACA389034578MYH7c.5738C>T (p.Ala1913Val)
dbSNP gnomAD v2
14g.23413811G>CCA389034580MYH7c.5738C>G (p.Ala1913Gly)
14g.23413811G=CA2123458218MYH7c.5738C= (p.Ala1913=)
14g.23413811G>TCA389034579MYH7c.5738C>A (p.Ala1913Asp)
14g.23413812C>ACA389034581MYH7c.5737G>T (p.Ala1913Ser)
14g.23413812C=CA2123458224MYH7c.5737G= (p.Ala1913=)
14g.23413812C>GCA389034582MYH7c.5737G>C (p.Ala1913Pro)
14g.23413812C>TCA048119MYH7c.5737G>A (p.Ala1913Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>ACA016427MYH7c.5736C>T (p.Ile1912=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>CCA389034583MYH7c.5736C>G (p.Ile1912Met)
14g.23413813G=CA2123458229MYH7c.5736C= (p.Ile1912=)
14g.23413813G>TCA485616119MYH7c.5736C>A (p.Ile1912=)
dbSNP
14g.23413814delCA2573053876MYH7c.5735del (p.Ile1912ThrfsTer21)
ClinVar dbSNP
14g.23413814A=CA2123458232MYH7c.5735T= (p.Ile1912=)
14g.23413814A>CCA389034584MYH7c.5735T>G (p.Ile1912Ser)
14g.23413814A>GCA389034585MYH7c.5735T>C (p.Ile1912Thr)
14g.23413814A>TCA389034586MYH7c.5735T>A (p.Ile1912Asn)
ClinVar dbSNP
14g.23413815T>ACA389034587MYH7c.5734A>T (p.Ile1912Phe)
ClinVar dbSNP gnomAD v4
14g.23413815T>CCA389034588MYH7c.5734A>G (p.Ile1912Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413815T>GCA389034589MYH7c.5734A>C (p.Ile1912Leu)
14g.23413815T=CA2123458238MYH7c.5734A= (p.Ile1912=)
14g.23413816G>ACA485616121MYH7c.5733C>T (p.Asp1911=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413816G>CCA389034590MYH7c.5733C>G (p.Asp1911Glu)
14g.23413816G=CA2123458263MYH7c.5733C= (p.Asp1911=)
14g.23413816G>TCA389034591MYH7c.5733C>A (p.Asp1911Glu)
14g.23413817T>ACA389034592MYH7c.5732A>T (p.Asp1911Val)
14g.23413817T>CCA389034594MYH7c.5732A>G (p.Asp1911Gly)
14g.23413817T>GCA389034593MYH7c.5732A>C (p.Asp1911Ala)
14g.23413818C>ACA389034595MYH7c.5731G>T (p.Asp1911Tyr)
COSMIC
14g.23413818C>GCA389034597MYH7c.5731G>C (p.Asp1911His)
14g.23413818C>TCA389034596MYH7c.5731G>A (p.Asp1911Asn)
14g.23413819delCA2800863467MYH7c.5731del (p.Asp1911ThrfsTer22)
14g.23413819C>ACA485616122MYH7c.5730G>T (p.Ala1910=)
14g.23413819C=CA2123458271MYH7c.5730G= (p.Ala1910=)
14g.23413819C>GCA485616124MYH7c.5730G>C (p.Ala1910=)
14g.23413819C>TCA048097MYH7c.5730G>A (p.Ala1910=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>ACA389034598MYH7c.5729C>T (p.Ala1910Val)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>CCA389034599MYH7c.5729C>G (p.Ala1910Gly)
14g.23413820G=CA2123458286MYH7c.5729C= (p.Ala1910=)
14g.23413820G>TCA389034600MYH7c.5729C>A (p.Ala1910Glu)
14g.23413821C>ACA389034601MYH7c.5728G>T (p.Ala1910Ser)
14g.23413821C>GCA389034602MYH7c.5728G>C (p.Ala1910Pro)

Number of alleles fetched